JPH10306006A - Herbicide composition - Google Patents

Herbicide composition

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Publication number
JPH10306006A
JPH10306006A JP9115699A JP11569997A JPH10306006A JP H10306006 A JPH10306006 A JP H10306006A JP 9115699 A JP9115699 A JP 9115699A JP 11569997 A JP11569997 A JP 11569997A JP H10306006 A JPH10306006 A JP H10306006A
Authority
JP
Japan
Prior art keywords
parts
weeds
fluthiamide
fluoro
flumioxazine
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP9115699A
Other languages
Japanese (ja)
Other versions
JP4003252B2 (en
Inventor
Nobuaki Mito
信彰 水戸
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP11569997A priority Critical patent/JP4003252B2/en
Priority to ARP980102062A priority patent/AR012651A1/en
Priority to US09/071,540 priority patent/US6001774A/en
Priority to CNB981087728A priority patent/CN1152610C/en
Priority to BRPI9801579-6A priority patent/BR9801579B1/en
Publication of JPH10306006A publication Critical patent/JPH10306006A/en
Application granted granted Critical
Publication of JP4003252B2 publication Critical patent/JP4003252B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

PROBLEM TO BE SOLVED: To obtain a herbicide composition, especially one suitable for controlling weeds in soybean fields. SOLUTION: This herbicide composition contains N-(7-fluoro-3,4-dihydro-3- oxo-4 bromo-2-ynyl-2H-1,4-benzoxazin-6-yl)cyclohex-1-ene-1,2-dicarboxamide and 4'-fluoro-N-isopropyl-2-(5-trifluoromethyl-1,3,4-thiadiazol-2-yloxy)ac etanilide as active ingredients, is capable of effectively killing various weeds emerging in crop land and non-crop land by application to soil or weeds, has synergistically increased herbicidal effects in comparison with their separate use, further enlarges a herbicidal spectrum and is capable of selectively controlling a wide range of weeds particularly causing a problem in soybean fields.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は除草剤組成物に関す
るものである。
[0001] The present invention relates to a herbicidal composition.

【0002】[0002]

【従来の技術および発明が解決しようとする課題】現
在、数多くの除草剤が市販され、 使用されているが、防
除の対象となる雑草は種類も多く、発生も長期間にわた
るため、より除草効果が高く、幅広い殺草スペクトラム
を有し、かつ作物には安全な除草剤が求められている。
2. Description of the Related Art At present, a large number of herbicides are commercially available and used. Therefore, there is a demand for safe herbicides in crops, which have a wide spectrum of herbicides and which have high cropping rates.

【0003】[0003]

【課題を解決するための手段】本発明者は優れた除草剤
を見出すべく鋭意検討した結果、N−(7−フルオロ−
3,4−ジヒドロ−3−オキソ−4−プロプ−2−イニ
ル−2H−1,4−ベンズオキサジン−6−イル)シク
ロヘキサ−1−エン−1,2−ジカルボキサミド(一般
名フルミオキサジン、以下フルミオキサジンと記す)と
4’−フルオロ−N−イソプロピル−2−(5−トリフ
ルオロメチル−1、3、4−チアジアゾ−ル−2−イル
オキシ)アセトアニリド(一般名フルチアミド、以下フ
ルチアミドと記す)とを有効成分として含有する除草剤
組成物を、土壌又は雑草に処理することにより、農耕地
あるいは非農耕地に発生する種々の雑草を効果的に除草
でき、しかもその除草効力は、それらを単独で用いる場
合に比較して相乗的に増大し、更に殺草スペクトルが拡
大し、特にダイズ畑において問題となる広範囲の雑草を
選択的に除草できることを見出し、本発明に至った。即
ち、本発明はフルミオキサジンとフルチアミドとを有効
成分として含有する除草剤組成物(以下、本発明組成物
と記す)を提供する。
The present inventors have conducted intensive studies to find an excellent herbicide and found that N- (7-fluoro-
3,4-dihydro-3-oxo-4-prop-2-ynyl-2H-1,4-benzoxazin-6-yl) cyclohex-1-ene-1,2-dicarboxamide (generic name flumioxazine, hereinafter Flumioxazine) and 4'-fluoro-N-isopropyl-2- (5-trifluoromethyl-1,3,4-thiadiazol-2-yloxy) acetanilide (generic name fluthiamide, hereinafter referred to as fluthiamide). By treating the herbicidal composition containing as an active ingredient a soil or a weed, various weeds generated on an agricultural land or a non-agricultural land can be effectively herbicidal. It increases synergistically and broadens the weed killing spectrum compared to when used, and can selectively remove a wide range of weeds, which are particularly problematic in soybean fields. This led to the present invention. That is, the present invention provides a herbicidal composition (hereinafter, referred to as the present composition) containing flumioxazine and fluthiamide as active ingredients.

【0004】[0004]

【発明の実施の形態】本発明組成物に於いて、一方の有
効成分であるフルミオキサジンはThe Pestic
ide Manual 10版(Crop Prote
ction Publication発行、 1994
年)489頁に記載の化合物である。また、他方の有効
成分であるフルチアミドはBrighton Crop
Protection Conference We
eds−1995 Proceedings Volu
me 1(The British Crop Pro
tection Council発行 1995年)4
4頁に記載の化合物である。
BEST MODE FOR CARRYING OUT THE INVENTION In the composition of the present invention, flumioxazin, one of the active ingredients, is used in The Pestic.
ide Manual 10th edition (Crop Prote
Ction Publication, 1994
(Year) p. 489. Fluthiamide, the other active ingredient, is available from Brighton Crop.
Protection Conference We
eds-1995 Proceedings Volu
me 1 (The British Crop Pro
Tissue Council published 1995) 4
Compounds described on page 4.

【0005】本発明組成物は、広範囲の雑草に対し除草
活性を有し、また作物との選択性にも富むことから、除
草剤として優れている。殊に、ダイズ畑における主要な
雑草、例えばソバカズラ、サナエタデ、アメリカサナエ
タデ、スベリヒユ、シロザ、アオゲイトウ、ノハラガラ
シ、アメリカツノクサネム、エビスグサ、イチビ、アメ
リカキンゴジカ、アメリカアサガオ、マルバアサガオ、
マルバアメリカアサガオ、ヨウシュチョウセンアサガ
オ、イヌホオズキ、オナモミ、ヒマワリ、セイヨウヒル
ガオ、トウダイグサ、アメリカセンダングサ、ブタクサ
等の双子葉植物および、イヌビエ、エノコログサ、アキ
ノエノコログサ、キンノエノコロ、メヒシバ、オヒシ
バ、セイバンモロコシ、シバムギ、シャッタ−ケ−ン等
の単子葉植物に対し除草活性を発揮する一方、作物であ
るダイズやダイズの後作物であるトウモロコシに対して
問題となるような薬害を生じない。また、本発明組成物
は、通常の耕起栽培の他、不耕起栽培に於いても優れた
除草活性を発揮し得る。
The composition of the present invention is excellent as a herbicide because it has herbicidal activity against a wide range of weeds and has high selectivity to crops. In particular, the main weeds in soybean fields, such as buckwheat, Sanaetada, Sasaenada, Suzurigyu, Shiroza, Aogetou, Noharagarashi, Utsunoxanem, Ebisugusa, Ichibi, American stag, American morning glory, Malva Asagao,
Malva American morning glory; While exhibiting herbicidal activity against monocotyledonous plants such as-soybean, it does not cause harmful damage to soybean as a crop or corn as a crop after soybean. In addition, the composition of the present invention can exhibit excellent herbicidal activity not only in ordinary tillage cultivation but also in no-tillage cultivation.

【0006】本発明組成物において、有効成分としての
フルミオキサジンとフルチアミドの混合割合は、通常、
重量比で1:0.1〜1000の範囲である。
In the composition of the present invention, the mixing ratio of flumioxazine and fluthiamide as active ingredients is usually
The weight ratio is in the range of 1: 0.1 to 1,000.

【0007】本発明組成物は通常、固体担体、液体担体
等と混合し、必要により界面活性剤、その他の製剤用補
助剤等を添加して、乳剤、水和剤、懸濁剤、粒剤等に製
剤化して用いられる。これらの製剤中に於いて、フルミ
オキサジンとフルチアミドとの含有量は、通常0.5〜
90重量%、好ましくは1〜80重量%の範囲である。
The composition of the present invention is usually mixed with a solid carrier, a liquid carrier and the like, and, if necessary, added with a surfactant and other auxiliaries for preparation. Etc. and used as a formulation. In these preparations, the content of flumioxazine and fluthiamide is usually 0.5 to
It is in the range of 90% by weight, preferably 1-80% by weight.

【0008】製剤化するに際し、用いられる固体担体と
しては、例えば粘土類(カオリナイト、珪藻土、合成含
水酸化珪素、フバサミクレ−、ベントナイト、酸性白土
等)、タルク、その他の無機鉱物(セリサイト、石英粉
末、硫黄粉末、活性炭、炭酸カルシウム等)化学肥料
(硫安、燐安、硝安、塩安、尿素等)などの微粉末や粒
状物が挙げられ、液体担体としては、例えば水、アルコ
−ル類(メタノ−ル、エタノ−ル等)、ケトン類(アセ
トン、メチルエチルケトン、シクロヘキサノン等)、芳
香族炭化水素類(トルエン、キシレン、エチルベンゼ
ン、メチルナフタレン等)、非芳香族炭化水素類(ヘキ
サン、シクロヘキサン、ケロシン等)、エステル類(酢
酸エチル、酢酸ブチル等)、ニトリル類(アセトニトリ
ル、イソブチロニトリル等)、エ−テル類(ジオキサ
ン、ジイソプロピルエ−テル等)、酸アミド類(ジメチ
ルホルムアミド、ジメチルアセトアミド等)、ハロゲン
化炭化水素類(ジクロロエタン、トリクロロエチレン
等)などが挙げられる。
[0008] The solid carrier used in the preparation includes, for example, clays (kaolinite, diatomaceous earth, synthetic hydrous silicon oxide, fubasamikure, bentonite, acid clay, etc.), talc, and other inorganic minerals (sericite, quartz) Powder, sulfur powder, activated carbon, calcium carbonate, etc.) Fine powders and granular materials such as fertilizers (ammonium sulfate, ammonium phosphate, ammonium nitrate, salt ammonium chloride, urea, etc.), and liquid carriers such as water, alcohols (E.g., methanol, ethanol), ketones (e.g., acetone, methyl ethyl ketone, cyclohexanone), aromatic hydrocarbons (e.g., toluene, xylene, ethylbenzene, methylnaphthalene), non-aromatic hydrocarbons (e.g., hexane, cyclohexane, etc.) Kerosene, etc.), esters (ethyl acetate, butyl acetate, etc.), nitriles (acetonitrile, isobutyronitrile) Etc.), e - ethers (dioxane, diisopropyl et - ether, etc.), acid amides (dimethylformamide, dimethylacetamide), halogenated hydrocarbons (dichloroethane, trichlorethylene, etc.) and the like.

【0009】界面活性剤としては、例えばアルキル硫酸
エステル類、アルキルスルホン酸塩、アルキルアリ−ル
スルホン酸塩、アルキルアリ−ルエ−テル類およびその
ポリオキシエチレン化物、ポリエチレングリコ−ルエ−
テル類、多価アルコ−ルエステル類、糖アルコ−ル誘導
体などが挙げられる。その他の製剤用補助剤としては、
例えばカゼイン、ゼラチン、多糖類(澱粉、アラビアガ
ム、セルロ−ス誘導体、アルギン酸等)、リグニン誘導
体、ベントナイト、合成水溶性高分子(ポリビニルアル
コ−ル、ポリビニルピロリドン、ポリアクリル酸等)な
どの固着剤や分散剤、PAP(酸性リン酸イソプロピ
ル)、BHT(2、6−tert−ブチル−4−メチル
フェノ−ル)、BHA(2−/3−tert−ブチル−
4−メトキシフェノ−ル)、植物油、鉱物油、脂肪酸、
脂肪酸エステルなどの安定剤が挙げられる。
Examples of the surfactant include alkyl sulfates, alkyl sulfonates, alkyl aryl sulfonates, alkyl aryl ethers and polyoxyethylenates thereof, and polyethylene glycol ethers.
Examples include ters, polyhydric alcohol esters, and sugar alcohol derivatives. Other formulation aids include:
For example, fixing agents such as casein, gelatin, polysaccharides (starch, gum arabic, cellulose derivatives, alginic acid, etc.), lignin derivatives, bentonite, synthetic water-soluble polymers (polyvinyl alcohol, polyvinylpyrrolidone, polyacrylic acid, etc.). And dispersant, PAP (isopropyl isopropyl phosphate), BHT (2,6-tert-butyl-4-methylphenol), BHA (2- / 3-tert-butyl-
4-methoxyphenol), vegetable oil, mineral oil, fatty acid,
Stabilizers such as fatty acid esters are included.

【0010】本発明組成物は、夫々の有効成分を上述の
製剤手法により製剤した後、これらを混合することによ
り調製することもできる。このようにして製剤化された
本発明組成物は、そのままでまたは水等で希釈して土壌
又は植物体に施用される。本発明組成物は、さらに、他
の除草剤と混合して用いることにより除草効力の増強を
期待でき、さらに殺虫剤、殺菌剤、植物生長調節剤、肥
料、土壌改良剤等と併用することもできる。
[0010] The composition of the present invention can also be prepared by formulating each active ingredient by the above-mentioned formulation technique and then mixing them. The composition of the present invention thus formulated is applied to soil or a plant as it is or after diluted with water or the like. The composition of the present invention can further be expected to enhance herbicidal efficacy by being used in combination with other herbicides, and can also be used in combination with insecticides, fungicides, plant growth regulators, fertilizers, soil improvers, and the like. it can.

【0011】本発明組成物の施用量は、有効成分化合物
であるフルミオキサジンとフルチアミドの混合比、気象
条件、製剤形態、施用時期、施用方法、施用場所、防除
対象雑草、対象作物により変わり得るが、1ヘクタ−ル
当り有効成分化合物の合計量として、通常5〜5000
gである。乳剤、水和剤、懸濁剤等は、その所定量を1
ヘクタ−ル当り通常100〜1000リットルの水で希
釈して施用し、粒剤等は通常何ら希釈することなく、そ
のまま施用する。
The application rate of the composition of the present invention may vary depending on the mixing ratio of flumioxazine and fluthiamide, which are the active ingredient compounds, weather conditions, preparation form, application time, application method, application place, weeds to be controlled, and target crops. The total amount of the active ingredient compound per hectare is usually 5 to 5000
g. For emulsions, wettable powders, suspensions, etc.
It is usually diluted with 100 to 1000 liters of water per hectare and applied. Granules and the like are usually applied without any dilution.

【0012】[0012]

【実施例】以下、製剤例を示す。以下の例において部は
重量部を表す。 製剤例1 フルミオキサジン5部、フルチアミド40部、リグニン
スルホン酸カルシウム3部、ラウリル硫酸ナトリウム2
部および合成含水酸化珪素50部をよく粉砕混合して水
和剤を得る。 製剤例2 フルミオキサジン8部、フルチアミド64部、リグニン
スルホン酸カルシウム3部、ラウリル硫酸ナトリウム2
部および合成含水酸化珪素23部をよく粉砕混合して水
和剤を得る。 製剤例3 フルミオキサジン40部、フルチアミド40部、リグニ
ンスルホン酸カルシウム3部、ラウリル硫酸ナトリウム
2部および合成含水酸化珪素15部をよく粉砕混合して
水和剤を得る。 製剤例4 フルミオキサジン25部、フルチアミド10部、リグニ
ンスルホン酸カルシウム3部、ラウリル硫酸ナトリウム
2部および合成含水酸化珪素60部をよく粉砕混合して
水和剤を得る。 製剤例5 フルミオキサジン3部、フルチアミド24部、ポリオキ
シエチレンソルビタンモノオレエ−ト3部、CMC(カ
ルボキシメチルセルロ−ス)3部および水67部を混合
し、粒度が5ミクロン以下になるまで湿式粉砕して懸濁
剤を得る。 製剤例6 フルミオキサジン5部、フルチアミド40部、ポリオキ
シエチレンソルビタンモノオレエ−ト3部、CMC(カ
ルボキシメチルセルロ−ス)3部および水49部を混合
し、粒度が5ミクロン以下になるまで湿式粉砕して懸濁
剤を得る。 製剤例7 フルミオキサジン20部、フルチアミド20部、ポリオ
キシエチレンソルビタンモノオレエ−ト3部、CMC
(カルボキシメチルセルロ−ス)3部および水54部を
混合し、粒度が5ミクロン以下になるまで湿式粉砕して
懸濁剤を得る。 製剤例8 フルミオキサジン30部、フルチアミド10部、ポリオ
キシエチレンソルビタンモノオレエ−ト3部、CMC
(カルボキシメチルセルロ−ス)3部および水54部を
混合し、粒度が5ミクロン以下になるまで湿式粉砕して
懸濁剤を得る。
[Examples] Formulation examples are shown below. In the following examples, parts represent parts by weight. Formulation Example 1 Flumioxazine 5 parts, Fluthiamide 40 parts, lignin sulfonate calcium 3 parts, sodium lauryl sulfate 2
Parts and 50 parts of synthetic hydrous silicon oxide are thoroughly pulverized and mixed to obtain a wettable powder. Formulation Example 2 Flumioxazine 8 parts, fluthiamide 64 parts, calcium lignin sulfonate 3 parts, sodium lauryl sulfate 2
Parts and 23 parts of synthetic hydrous silicon oxide are pulverized and mixed well to obtain a wettable powder. Formulation Example 3 40 parts of flumioxazin, 40 parts of fluthiamide, 3 parts of calcium ligninsulfonate, 2 parts of sodium lauryl sulfate and 15 parts of synthetic hydrous silicon oxide are thoroughly pulverized and mixed to obtain a wettable powder. Formulation Example 4 25 parts of flumioxazine, 10 parts of fluthiamide, 3 parts of calcium ligninsulfonate, 2 parts of sodium lauryl sulfate and 60 parts of synthetic hydrous silicon oxide are thoroughly pulverized and mixed to obtain a wettable powder. Formulation Example 5 3 parts of flumioxazine, 24 parts of fluthiamide, 3 parts of polyoxyethylene sorbitan monooleate, 3 parts of CMC (carboxymethyl cellulose) and 67 parts of water are mixed until the particle size becomes 5 microns or less. The suspension is obtained by wet grinding. Formulation Example 6 5 parts of flumioxazine, 40 parts of fluthiamide, 3 parts of polyoxyethylene sorbitan monooleate, 3 parts of CMC (carboxymethyl cellulose) and 49 parts of water are mixed until the particle size becomes 5 microns or less. The suspension is obtained by wet grinding. Formulation Example 7 Flumioxazine 20 parts, Fluthiamide 20 parts, polyoxyethylene sorbitan monooleate 3 parts, CMC
3 parts of (carboxymethyl cellulose) and 54 parts of water are mixed and wet-pulverized until the particle size becomes 5 μm or less to obtain a suspending agent. Formulation Example 8 30 parts flumioxazine, 10 parts fluthiamide, 3 parts polyoxyethylene sorbitan monooleate, CMC
3 parts of (carboxymethyl cellulose) and 54 parts of water are mixed and wet-pulverized until the particle size becomes 5 μm or less to obtain a suspending agent.

【0013】以下に試験例を示す。下記試験例に於い
て、除草効力の評価は、調査時の供試雑草の出芽または
生育の状態が無処理のそれと比較して全く乃至ほとんど
違いがないものを「0」とし、供試植物が完全枯死また
は出芽もしくは生育が完全に抑制されているものを「1
0」として、0〜10の11段階に区分し、0、1、
2、3、4、5、6、7、8、9、10で示す。該評価
に於いて、除草効力の評価値「7」以上は顕著な除草効
力を発揮していることを意味し、評価値「5」以下は除
草効力が不充分であることを意味する。薬害の評価は、
薬害がほとんど認められない場合は「無害」、軽度の薬
害が認められる場合は「小」、中程度の薬害が認められ
る場合は「中」、強度の薬害が認められる場合は「大」
で示す。 試験例1 フルミオキサジン2.5部、トキサノンP8L(三洋化
成工業株式会社登録商標)16.25部、シクロヘキサ
ノン81.25部をよく混合して得られるフルミオキサ
ジンの乳剤及びフルチアミド2.5部、トキサノンP8
L(三洋化成工業株式会社登録商標)16.25部、シ
クロヘキサノン81.25部をよく混合して得られるフ
ルチアミドの乳剤を用意した。縦18cm、横20c
m、深さ7.5cmのプラスチックポットに畑地土壌を
詰めダイズ、イチビ、アメリカアサガオ、アメリカキン
ゴジカ、オナモミ、サナエタデ、シロバナチョウセンア
サガオ、スベリヒユ、メヒシバ、アキノエノコログサ、
イヌビエを播種した。次いで、上記各乳剤及びこれらの
混合物の所定量を、下表1の薬量になるように水で希釈
し、小型噴霧器で土壌表面に均一に散布した。処理後温
室内で育成し、11日目にダイズに対する安全性、雑草
に対する除草効力を調査した。結果を(表1)に示す。
Test examples are shown below. In the following test examples, the evaluation of the herbicidal efficacy was made such that the emergence or growth state of the test weed at the time of the survey showed no or little difference compared to that of the untreated test weed, and the test plant was evaluated as “0”. Those that are completely killed or whose budding or growth is completely suppressed are referred to as "1.
0 ”as 11 levels from 0 to 10, 0, 1,
2, 3, 4, 5, 6, 7, 8, 9, and 10. In this evaluation, an evaluation value of "7" or more of the herbicidal effect means that a remarkable herbicidal effect is exhibited, and an evaluation value of "5" or less means that the herbicidal effect is insufficient. Evaluation of phytotoxicity
"Harmless" when little phytotoxicity is found, "Small" when mild phytotoxicity is found, "Medium" when moderate phytotoxicity is found, "Large" when severe phytotoxicity is found
Indicated by Test Example 1 Flumioxazine 2.5 parts, Toxanone P8L (Registered trademark of Sanyo Chemical Industry Co., Ltd.) 16.25 parts, Emulsion of flumioxazine and fluthiamide 2.5 parts obtained by thoroughly mixing 81.25 parts of cyclohexanone, Toxanone P8
L (Sanyo Kasei Kogyo KK) (16.25 parts) and 81.25 parts of cyclohexanone were mixed well to prepare a fluthiamide emulsion. 18cm in height, 20c in width
m, 7.5 cm deep plastic pots filled with field soil, soybeans, strawberries, American morning glory, American sika deer, Onami fir, Sanaetadae, Shirobananasenasaagao, Suberihyu, Mehishiba, Aquinoenokologa,
Dog millet was sown. Next, a predetermined amount of each of the above-mentioned emulsions and a mixture thereof was diluted with water so as to have a dose as shown in Table 1 below, and uniformly sprayed on the soil surface with a small sprayer. After treatment, the plants were grown in a greenhouse, and on the eleventh day, the safety against soybeans and the herbicidal efficacy against weeds were examined. The results are shown in (Table 1).

【表1】 [Table 1]

【0014】[0014]

【発明の効果】本発明組成物を用いることにより、畑地
雑草等、特に、ダイズ畑における広範囲の雑草を選択的
に除草できる。
EFFECT OF THE INVENTION By using the composition of the present invention, a wide range of weeds in a soybean field, particularly in a soybean field, can be selectively removed.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】N−(7−フルオロ−3,4−ジヒドロ−
3−オキソ−4−プロプ−2−イニル−2H−1,4−
ベンズオキサジン−6−イル)シクロヘキサ−1−エン
−1,2−ジカルボキサミドと4’−フルオロ−N−イ
ソプロピル−2−(5−トリフルオロメチル−1、3、
4−チアジアゾ−ル−2−イルオキシ)アセトアニリド
とを有効成分として含有することを特徴とする除草剤組
成物。
(1) N- (7-fluoro-3,4-dihydro-)
3-oxo-4-prop-2-ynyl-2H-1,4-
Benzoxazin-6-yl) cyclohex-1-ene-1,2-dicarboxamide and 4'-fluoro-N-isopropyl-2- (5-trifluoromethyl-1,3,
A herbicidal composition comprising 4-thiadiazol-2-yloxy) acetanilide as an active ingredient.
【請求項2】ダイズ畑における雑草を防除するための請
求項1に記載の除草剤組成物。
2. The herbicidal composition according to claim 1, for controlling weeds in a soybean field.
JP11569997A 1997-05-06 1997-05-06 Herbicidal composition Expired - Fee Related JP4003252B2 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP11569997A JP4003252B2 (en) 1997-05-06 1997-05-06 Herbicidal composition
ARP980102062A AR012651A1 (en) 1997-05-06 1998-05-04 HERBICIDE COMPOSITION AND WEEDLESS METHOD USING THE SAME.
US09/071,540 US6001774A (en) 1997-05-06 1998-05-04 Herbicidal composition
CNB981087728A CN1152610C (en) 1997-05-06 1998-05-05 Herbicidal composition
BRPI9801579-6A BR9801579B1 (en) 1997-05-06 1998-05-05 Herbicidal composition comprising flumioxazin and flutiamide, use thereof and process for weeding employing said composition.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11569997A JP4003252B2 (en) 1997-05-06 1997-05-06 Herbicidal composition

Publications (2)

Publication Number Publication Date
JPH10306006A true JPH10306006A (en) 1998-11-17
JP4003252B2 JP4003252B2 (en) 2007-11-07

Family

ID=14669050

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11569997A Expired - Fee Related JP4003252B2 (en) 1997-05-06 1997-05-06 Herbicidal composition

Country Status (1)

Country Link
JP (1) JP4003252B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010163411A (en) * 2008-12-17 2010-07-29 Bayer Cropscience Ag Herbicidal composition
JP4806518B2 (en) * 2001-11-27 2011-11-02 バレント バイオサイエンシス コーポレーション Enhanced herbicidal composition

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4806518B2 (en) * 2001-11-27 2011-11-02 バレント バイオサイエンシス コーポレーション Enhanced herbicidal composition
JP2010163411A (en) * 2008-12-17 2010-07-29 Bayer Cropscience Ag Herbicidal composition

Also Published As

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